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Synthesis of a Biologically Important Adenosine Triphosphate Analogue, ApppD
[Image: see text] The chemical synthesis of a adenosine triphosphate analogue, 1-adenosin-5′-yl 3-(3-methylbut-2-enyl) triphosphoric acid diester (ApppD), is described. ApppD is known to be an active metabolite of the mevalonate pathway in the human body like its structural isomer isopentenyl ester...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044877/ https://www.ncbi.nlm.nih.gov/pubmed/30023676 http://dx.doi.org/10.1021/acsomega.7b00531 |
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author | Turhanen, Petri A. |
author_facet | Turhanen, Petri A. |
author_sort | Turhanen, Petri A. |
collection | PubMed |
description | [Image: see text] The chemical synthesis of a adenosine triphosphate analogue, 1-adenosin-5′-yl 3-(3-methylbut-2-enyl) triphosphoric acid diester (ApppD), is described. ApppD is known to be an active metabolite of the mevalonate pathway in the human body like its structural isomer isopentenyl ester of ATP (ApppI). Very recently, ApppI has been found to possess novel function(s); now it will also be possible to examine the effects of ApppD more precisely because it can be synthesized in reasonable amounts. 1-Adenosin-5′-yl 3-(3-methylbut-2-enyl) diphosphoric acid diester (AppD; a adenosine diphosphate analogue) was also isolated from the synthesis mixture. Both ApppD and AppD were characterized by (1)H, (13)C, (31)P NMR and mass spectrometry methods. |
format | Online Article Text |
id | pubmed-6044877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-60448772018-07-16 Synthesis of a Biologically Important Adenosine Triphosphate Analogue, ApppD Turhanen, Petri A. ACS Omega [Image: see text] The chemical synthesis of a adenosine triphosphate analogue, 1-adenosin-5′-yl 3-(3-methylbut-2-enyl) triphosphoric acid diester (ApppD), is described. ApppD is known to be an active metabolite of the mevalonate pathway in the human body like its structural isomer isopentenyl ester of ATP (ApppI). Very recently, ApppI has been found to possess novel function(s); now it will also be possible to examine the effects of ApppD more precisely because it can be synthesized in reasonable amounts. 1-Adenosin-5′-yl 3-(3-methylbut-2-enyl) diphosphoric acid diester (AppD; a adenosine diphosphate analogue) was also isolated from the synthesis mixture. Both ApppD and AppD were characterized by (1)H, (13)C, (31)P NMR and mass spectrometry methods. American Chemical Society 2017-06-21 /pmc/articles/PMC6044877/ /pubmed/30023676 http://dx.doi.org/10.1021/acsomega.7b00531 Text en Copyright © 2017 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Turhanen, Petri A. Synthesis of a Biologically Important Adenosine Triphosphate Analogue, ApppD |
title | Synthesis of a Biologically Important Adenosine Triphosphate
Analogue, ApppD |
title_full | Synthesis of a Biologically Important Adenosine Triphosphate
Analogue, ApppD |
title_fullStr | Synthesis of a Biologically Important Adenosine Triphosphate
Analogue, ApppD |
title_full_unstemmed | Synthesis of a Biologically Important Adenosine Triphosphate
Analogue, ApppD |
title_short | Synthesis of a Biologically Important Adenosine Triphosphate
Analogue, ApppD |
title_sort | synthesis of a biologically important adenosine triphosphate
analogue, apppd |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044877/ https://www.ncbi.nlm.nih.gov/pubmed/30023676 http://dx.doi.org/10.1021/acsomega.7b00531 |
work_keys_str_mv | AT turhanenpetria synthesisofabiologicallyimportantadenosinetriphosphateanalogueapppd |